Beyond compliance in Bologna: sharing knowledge across borders
On 30 September and 1 October, GBA Key2Compliance colleagues Emily Malmberg and Maria Nordlinder travelled to Bologna to participate as invited speakers at Complife’s annual MDG Health Matters – Medical Device Governance Forum: Beyond Compliance. Complife, part of GBA Group, brought together representatives from across the medical device and IVD industry, including the Italian Ministry […]
EUDAMED registration: Are you ready for the 28 November 2026 deadline?
The next important EUDAMED deadline is approaching. By 28 November 2026, manufacturers must ensure that applicable legacy devices and other devices covered by the transitional registration requirements are registered in EUDAMED. Is your organisation prepared? Since 28 May 2026, the use of four EUDAMED modules has become mandatory under the EU Medical Device Regulation (MDR) […]